Reversible surface aggregation in pore formation by pardaxin

Biophysical Journal

Volumn 70, Issue 6, 1996, Pages 2502-2512

  Rapaport, Doron ^a   Peled, Ruth ^a   Nir, Shlomo ^a   Shai, Yechiel ^a,b  

^a HEBREW UNIVERSITY OF JERUSALEM   (Israel)

^b WEIZMANN INSTITUTE OF SCIENCE   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

CHOLESTEROL; PARDAXIN; PHOSPHATIDYLCHOLINE; PHOSPHATIDYLSERINE;

ARTICLE; LIPID MEMBRANE; MEMBRANE MODEL; MEMBRANE PERMEABILITY; MEMBRANE TRANSPORT; MEMBRANE VESICLE; PROTEIN AGGREGATION; PROTEIN LIPID INTERACTION; PROTEIN TRANSPORT; TEMPERATURE SENSITIVITY; TRANSPORT KINETICS;

EID: 0030025781     PISSN: 00063495     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-3495(96)79822-3     Document Type: Article

References (58)

1. Allen, T. M., and L. G. Cleland. 1980. Serum-induced leakage of liposome contents. Biochim. Biophys. Acta. 597:418-426.
2. Bentz, J., and S. Nir. 1981. Mass action kinetics and equilibria of reversible aggregation. J. Chem. Soc. Faraday Trans. 177:1249-1275.
3. Bentz, J., S. Nir, and D. G. Covell. 1988. Mass action kinetics of virus-cell aggregation and fusion. Biophys. J. 54:449-462.
4. Bentz, J., S. Nir, and J. Wilschut. 1983. Mass action kinetics of vesicle aggregation and fusion. Colloids Surf. 6:333-363.
5. Blatz, P. J., and A. V. Tobolsky. 1945. Note on the kinetics of systems manifesting simultaneous polimerization- dipolimerization phenomena. J. Phys. Chem. 49:77-80.
6. Boman, H. G. 1991. Antibacterial peptides: key components needed in immunity. Cell. 65:205-207.
7. Cheetham, J. J., R. M. Epand, M. Andrews, and T. D. Flanagan. 1990. Cholesterol sulfate inhibits the fusion of Sendai virus to biological and model membranes. J. Biol. Chem. 265:12404-12409.
8. Chen, R. F., and J. R. Knutson. 1988. Mechanism of fluorescence concentration quenching of carboxyfluorescein in liposomes: energy transfer to nonfluorescent dimers. Anal. Biochem. 172:61-77.
9. Christensen, B., J. Fink, R. B. Merrifield, and D. Mauzerall. 1988. Channel-forming properties of cecropins and related model compounds incorporated into planar lipid membranes. Proc. Natl. Acad. Sci. USA. 85:5072-5076.
10. Day, E. P., A. Y. W. Kwok, S. K. Hark, J. T. Ho, W. J. Vail, J. Bentz, and S. Nir. 1980. Reversibility of sodium-induced aggregation of sonicated phosphatidylserine vesicles. Proc. Natl. Acad. Sci. USA. 77:4026-4029.
11. Düzgiines, N., M. C. Pedroso de Lima, L. Stamatatos, D. Flasher, D. Alford, D. S. Friend, and S. Nir. 1992. Fusion activity and inactivation of influenza virus: kinetics of low pH-induced fusion with cultured cells. J. Gen. Virol. 73:27-37.
12. Düzgünes, N., and S. A. Shavnin. 1992. Membrane destabilization by N-terminal peptides of viral envelope proteins. J. Membr. Biol. 128: 71-80.
13. Epand, R. M., J. J. Cheetham, R. F. Epand, P. L. Yeagle, C. D. Richardson, A. Rockwell, and W. F. Degrado. 1992. Peptide models for the membrane destabilizing actions of viral fusion proteins. Biopolymers. 32: 309-314.
14. Fattal, E., S. Nir, R. A. Parente, and F. C. J. Szoka. 1994. pore forming peptides induce rapid phospholipid flip-flop in membranes. Biochemistry. 33:6721-6731.
15. Flory, P. J. 1939. Kinetics of polyesterification: a study of the effects of molecular weight and viscosity on reaction rate. J. Am. Chem. Soc. 61:3334-3340.
16. Frey, S., and L. K. Tamm. 1990. Membrane insertion and lateral diffusion of fluorescence-labelled cytochrome c oxidase subunit IV signal peptide in charged and uncharged phospholipid bilayers. Biochem. J. 272: 713-719.
17. Gazit, E., and Y. Shai. 1993. Structural characterization, membrane interaction, and specific assembly within phospholipid membranes of hydrophobic segments from Bacillus thuringiensis var. israelensis cytolytic toxin. Biochemistry. 32:12363-12371.
18. Ghosh, P., S. F. Mel, and R. M. Stroud. 1993. A carboxy-terminal fragment of colicin Ia forms ion channels. J. Membr. Biol. 134:85-92.
19. Harshman, S., P. Boquet, E. Duflot, J. E. Alouf, C. Montecucco, and E. Papini. 1989. Staphylococcal alpha-toxin: a study of membrane penetration and pore formation. J. Biol Chem. 264:14978-14984.
20. Hope, M. J., M. B. Bally, G. Webb, and P. R. Cullis. 1985. Production of large unilamellar vesicles by a rapid extrusion procedure. Characterization of size distribution, trapped volume and ability to maintain a membrane potential. Biochim. Biophys. Acta. 812:55-65.
21. Lazarovici, P., C. Edwards, G. Raghunathan, and H. R. Guy. 1992. Secondary structure, permeability and molecular modeling of pardaxin pores. J. Nat. Toxins. 1:1-15.
22. Lazarovici, P., and P. I. Lelkes. 1992. Pardaxin induces exocytosis in bovine adrenal medullary chromaffin cells independent of calcium. J. Pharmacol Exp. Ther. 263:1317-1326.
23. Lazarovici, P., N. Primor, and L. M. Loew. 1986. Purification and Poreforming activity of two hydrophobic polypeptides from the secretion of the Red Sea Moses sole (Pardachirus marmoratus). J. Biol. Chem. 261:16704-16713.
24. Lear, J. D., Z. R. Wasserman, and W. F. DeGrado. 1988. Synthetic amphiphilic peptide models for protein ion channels [and erratum in Science 1989 245:1437]. Science. 240:1177-1181.
25. Lewis, T., and H. M. McConnel. 1978. Model lipid bilayer membranes as target for antibody-desendent, cellular- and complement-mediated immune attack. Ann. N.Y. Acad. Sci. 308:124-136.
26. Martin, I., Q. F. Defrise, V. Mandieau, N. M. Nielsen, T. Saermark, A. Burny, R. Brasseur, J. M. Ruysschaert, and M. Vandenbranden. 1991. Fusogenic activity of SIV (simian immunodeficiency virus) peptides located in the GP32 NH2 terminal domain. Biochem. Biophys. Res. Commun. 175:872-879.
27. Matsuzaki, K., M. Fukui, N. Fujii, and K. Myajima. 1993. Permeabilization and morphological changes in phosphatidylglycerol bilayers induced by an antimicrobial peptide, Tachyplesrinl. Colloid Polym. Sci. 271: 901-908.
28. Merrifield, R. B., L. D. Vizioli, and H. G. Boman. 1982. Synthesis of the antibaterial peptide Cecropin A(1-33). Biochemistry. 21:5020-5031.
29. Nieva, J. L., S. Nir, A. Muga, F. M. Goni, and J. Wilschut. 1994. Interaction of the HIV-1 fusion peptide with phospholipid vesicles: different structural requirements for fusion and leakage. Biochemistry. 33:3201-3209.
30. Nir, S., J. Bentz, and A. R. J. Portis. 1980. Effect of cation concentrations and temperature on the rates of aggregation of acidic phospholipid vesicles: application to fusion. Adv. Chem. 188:75-106.
31. Nir, S., J. Bentz, J. Wilschut, and N. Duzgunes. 1983. Aggregation and fusion of phospholipid vesicles. Prog. Surf. Sci. 13:1-124.
32. Nir, S., K. Klappe, and D. Hoekstra. 1986. Kinetics and extent of fusion between Sendai virus and erythrocyte ghosts: application of a mass action kinetic model. Biochemistry. 25:2155-2161.
33. Nir, S., R. Peled, and K. Lee. 1994. Analysis of particle uptake by cells: binding to several receptors, equilibration time, endocytosis. Colloid Surf. 89:45-57.
34. Papahadjopoulos, D., K. Jacobson, S. Nir, and T. Isac. 1973. Phase transitions in phospholipid vesicles. Fluorescence polarization and permeability measurements concerning the effect of temperature and cholesterol. Biochim. Biophys. Acta. 311:330-348.
35. Parente, R. A., S. Nir, and J. Szoka F. C. 1990. Mechanism of leakage of phospholipid vesicle contents induced by the peptide GALA. Biochemistry. 29:8720-8728.
36. Peled, C. R., G. Braun, and S. Nir. 1995. Time of equilibration in reversible aggregation of particles. J. Colloid Interface Sci. 169:204-213.
37. Primor, N., J. Parness, and E. Zlotkin. 1978. Pardaxin: the toxic factor from the skin secretion of the flatfish Pardachirus marmoratus (Soleidae). In Toxins: Animal, Plant and Microbial. P. E. Rosenberg, editor. Pergamon Press, New York. 539.
38. Rafalski, M., A. Ortiz, A. Rockwell, G. L. van, J. D. Lear, W. F. DeGrado, and J. Wilschut. 1991. Membrane fusion activity of the influenza virus hemagglutinin: interaction of HA2 N-terminal peptides with phospholipid vesicles. Biochemistry. 30:10211-10220.
39. Rapaport, D., G. R. Hague, Y. Pouny, and Y. Shai. 1993. pH- and ionic strength-dependent fusion of phospholipid vesicles induced by pardaxin analogues or by mixtures of charge-reversed peptides. Biochemistry. 32:3291-3297.
40. Rapaport, D., S. Nir, and Y. Shai. 1994. Capacities of pardaxin analogues to induce fusion and leakage of negatively charged phospholipid vesicles are not necessarily correlated. Biochemistry. 33:12615-12624.
41. Rapaport, D., and Y. Shai. 1991. Interaction of fluorescently labeled pardaxin and its analogues with lipid bilayers. J. Biol. Chem. 266: 23769-23775.
42. Rapaport, D., and Y. Shai. 1992. Aggregation and organization of pardaxin in phospholipid membranes. A fluorescence energy transfer study. J. Biol. Chem. 267:6502-6509.
43. Rouser, B., A. Siakotos, and S. Fleischer. 1966. Quantitative analysis of phospholipid by thin layer chromatography and phosphorous analysis of spots. Lipids. 1:85-86.
44. Schwarz, G., and G. Beschiaschvili. 1989. Thermodynamic and kinetic studies on the association of melittin with a phospholipid bilayer. Biochim. Biophys. Acta. 979:82-90.
45. Schwarz, G., S. Stankowski, and V. Rizzo. 1986. Thermodynamic analysis of incorporation and aggregation in a membrane: application to the pore-forming peptide alamethicin. Biochim. Biophys. Acta. 861: 141-151.
46. Shai, Y. 1994. Pardaxin: channel formation by a shark repellant peptide from fish. Toxicology. 87:109-129.
47. Shai, Y., D. Bach, and A. Yanovsky. 1990. Channel formation properties of synthetic pardaxin and analogues. J. Biol. Chem. 265:20202-20209.
48. Shai, Y., J. Fox, C. Caratsch, Y. L. Shih, C. Edwards, and P. Lazarovici. 1988. Sequencing and synthesis of pardaxin, a polypeptide from the Red Sea Moses sole with ionophore activity. FEBS. Lett. 242:161-166.
49. Shai, Y., Y. R. Hadari, and A. Finkels. 1991. pH-dependent pore formation properties of pardaxin analogues. J. Biol. Chem. 266:22346-22354.
50. Smoluchowski, M. V. 1917. Versuch einer mathematischen Theorie der Koagulationskinetik Koloider Losungen. Z. Phis. Chem. Stochiometrie Vervandschaftsl. 92:129-168.
51. Spruce, A. E., A. Iwata, J. M. White, and W. Almers. 1989. Patch clamp studies of single cell-fusion events mediated by a viral fusion protein. Nature. 342:555-558.
52. Steiner, H., D. Andreu, and R. B. Merrifield. 1988. Binding and action of cecropin and cecropin analogues: antibacterial peptides from insects. Biochim. Biophys. Acta. 939:260-266.
53. Struck, K. D., D. Hoekstra, and R. E. Pagano. 1981. Use of resonance energy transfer to monitor membrane fusion. Biochemistry. 20: 4093-4099.
54. Szoka, F. C., and D. Papahadjopoulos. 1980. Comparative properties and methods of preparation of lipid vesicles (liposomes). Annu. Rev. Biophys. Bioeng. 9:467-508.
55. Weinstein, J. N., R. D. Klausner, T. Innerarity, E. Ralston, and R. Blumenthal. 1981. Phase transition release, a new approach to the interaction of proteins with lipid vesicles. Application to lipoproteins. Biochim. Biophys. Acta. 647:270-284.
56. White, J. M. 1992. Membrane fusion. Science. 258:917-924.
57. Wu, D., and A. I. Aronson. 1992. Localized mutagenesis defines regions of the Bacillus thuringiensis delta-endotoxin involved in toxicity and specificity. J. Biol. Chem. 267:2311-2317.
58. Zasloff, M. 1992. Antibiotic peptides as mediators of innate immunity. Curr. Opin. Immunol. 4:3-7.